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COMPLETED
NCT02884297
PHASE3

HexafluOride, a Contrast Agent for Placenta Echo-angiography

Sponsor: Centre Hospitalier Régional Metz-Thionville

View on ClinicalTrials.gov

Summary

The purpose of this study is to quantify the placental perfusion during the first trimester of pregnancy by 3D Doppler ultrasound angiography without a contrast agent and by ultrasound with a contrast agent: SonoVue®

Official title: Feasibility Study of the Measurement of the Placental Perfusion During the First Trimester of Pregnancy by 3D Doppler Echo-angiography With a Contrast Agent

Key Details

Gender

FEMALE

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

55

Start Date

2016-10-12

Completion Date

2019-09-30

Last Updated

2026-06-24

Healthy Volunteers

No

Conditions

Interventions

DRUG

Contrast agent: SonoVue®.

SonoVue® Injection: will be done through the peripheral venous way already set up by the anesthetist for its injection. None venous dedicated way will be established. The injection will take place when the woman will be under general anesthesia, ventilated and under constant cardio-respiratory monitoring.

Locations (2)

Chr Metz Thionville

Metz, France

CHRU de NANCY

Nancy, France